Method for Detecting the Presence of Target Bacteria or a Target Component Carbohydrate Antigen Thereof
a technology of target bacteria and carbohydrate antigen, which is applied in the field of detecting the presence of target bacteria or a target component carbohydrate antigen thereof, can solve the problems of cumbersome methodology, bacterial disease diagnosis and diagnosis often arrived at slowly and difficulty, and sputum may give false negative or false positiv
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example 1
Culture Conditions for Culturing the Target Carbohydrate Antigen
[0050]Haemophilus influenzae type b (ATCC #10211) was grown in supplemented Mueller Hinton broth at 37° C. with 5 percent CO2 for 24 hours without agitation.
[0051] The broth composition, per liter, was:
Acid hydrolyzate of casein17.5 g. Beef heart extract3.0 g.Starch1.5 g.
[0052] Supplements as follows were also present:
Hematin15 mg. / mLNAD (nicotine adenine dinucleotide)15 mg. / mLYeast extract 5 mg. / mL
[0053] The pH of this mixture was 7.3±0.1 as measured at 25° C.
example 2
Purification of Carbohydrate Antigen
[0054] After 24 hours, 1.82 g. of cetyltrimethylammonium bromide CAS #57-09-0 was dissolved in 30 mL of distilled water and the solution was added to 500 mL of broth supernatant to yield a final concentration of 0.01 M cetyltrimethylammonium bromide. The mixture was incubated in an ice bath with stirring for one hour and left at 4° C. overnight.
[0055] The mixture from Example 1 was centrifuged at 12,000 rpm and 4° C. for 20 minutes to yield a pellet and a supernatant. Both were collected and treated, respectively, as follows:
[0056] (1) The pellet was resuspended in 0.5 M NaCl with sonication and was then dropwise precipitated at 4° C. in ten times the resuspension volume of ethanol. The resulting solution was stored overnight at 4° C. to allow precipitation.
[0057] The solution was then centrifuged at 12,000 rpm for 20 minutes. The pellet was dissolved in distilled water and then dialyzed against distilled water in dialysis tubing having a mole...
example 3
Preparation of Affinity Column
[0061] Five mg. of lyophilized Haemophilus influenzae type b polysaccharide antigen was dissolved in 4.52 mL of distilled water and the pH was adjusted to 5-6 with HCl; 15.64 mg. of bovine serum albumen-hydrazine conjugate of pH 5-6 was then added, followed by mixing for three minutes.
[0062] 2.6 μg of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (“EDAC”) was dissolved in 100 μL of distilled water. 50 μL of this solution was added to the antigen / BSA-hydrazine conjugate solution, followed by three minutes of mixing. The balance of the EDAC solution was then added to this mixture followed by two hours of mixing at room temperature. The pH was then adjusted to 8 with NaOH and mixed for one hour at room temperature, followed by storage overnight at 4° C.
[0063] The next day the pH of the stored mixture was adjusted to 7 with HCl and a portion was subjected to the ELISA test, confirming its activity.
[0064] 2.12 mg. of the EDAC-treated antigen / BSA hydrazi...
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